The novel histone deacetylase inhibitor 4-Me2N-BAVAH differentially affects cell junctions between primary hepatocytes

Toxicology

Volumn 236, Issue 1-2, 2007, Pages 92-102

  Vinken, Mathieu ^a   Henkens, Tom ^a   Snykers, Sarah ^a   Lukaszuk, Aneta ^a   Tourwé, Dirk ^a   Rogiers, Vera ^a   Vanhaecke, Tamara ^a  

^a VRIJE UNIVERSITEIT BRUSSEL   (Belgium)

Author keywords

5 (4 Dimethylaminobenzoyl) aminovaleric acid hydroxamate; Adherens junction; Gap junction; Histone deacetylase inhibitor; Primary hepatocytes

Indexed keywords

5 (4 DIMETHYLAMINOBENZOYL) AMINOVALERIC ACID HYDROXAMATE; BETA CATENIN; CONNEXIN 26; CONNEXIN 32; CONNEXIN 43; HISTONE DEACETYLASE INHIBITOR; PLAKOGLOBIN; UNCLASSIFIED DRUG; UVOMORULIN;

ANIMAL CELL; ARTICLE; CELL JUNCTION; CELL VIABILITY; CELLULAR DISTRIBUTION; CONTROLLED STUDY; DRUG ACTIVITY; DRUG EFFECT; DRUG STRUCTURE; GAP JUNCTION; HOMEOSTASIS; LIVER CELL; NONHUMAN; PRIORITY JOURNAL; RAT;

ACETYLATION; ADHERENS JUNCTIONS; ANIMALS; CELL SURVIVAL; CELLS, CULTURED; CONNEXIN 43; CONNEXINS; GAP JUNCTIONS; GENE EXPRESSION REGULATION; HEPATOCYTES; HISTONE DEACETYLASES; HISTONES; HYDROXAMIC ACIDS; MALE; PENTANOIC ACIDS; RATS; RATS, SPRAGUE-DAWLEY;

RATTUS;

EID: 34248657000     PISSN: 0300483X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tox.2007.04.003     Document Type: Article

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